Peculiarities of the effect of antiepileptic drugs on seizures in mice with corneal kindling against the background of low-dose premedication with carbamazepine and sulthiame

Q3 Pharmacology, Toxicology and Pharmaceutics ScienceRise: Pharmaceutical Science Pub Date : 2023-06-30 DOI:10.15587/2519-4852.2023.265308
Y. Boiko, Yevhen Тantsura, I. Boiko, Liudmyla Tantsura
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Abstract

The aim. The aim of the study was to evaluate the effectiveness of antiepileptic drugs (AED) with a different mechanism of action against the background of prior use of low doses of carbamazepine and sultiam in the model of corneal kindling in mice. Materials and methods. The corneal kindling model in mice was used. The convulsive model was reproduced under the parallel preliminary administration of carbamazepine and sulthiame 30 minutes before electrostimulation. The anticonvulsant activity of AED (sulthiame, levetiracetam, carbamazepine, valproate, lamotrigine and retigabine) was studied under conditions after the formation of a stable syndrome of the generalised convulsive activity. Results and discussion. The administration of carbamazepine and sulthiame drugs modulates the activity of the cytochrome P450 enzyme system. Thus, carbamazepine in the dose of 7 and 12 mg/kg showed no significant anticonvulsant activity (the convulsive intensity – 4.42±0.25 points; 4.44±0.32 points) after its preliminary chronic administration, the same doses of carbamazepine showed a noticeable anticonvulsant effect in the control group of animals (3.52±0.26 points; 3.2±0.6 points, respectively). The anticonvulsant activity of lamotrigine changed both in the case of the preliminary chronic administration of an inducer (carbamazepine), and an inhibitor (sulthiame) of the cytochrome P450 system. Conclusion. Changes in the pharmacological effects of AED observed against the background of chronic administration of carbamazepine and sulthiame, in our opinion, may be due to both the modulation of the cytochrome P450 system and other groups of enzymes involved in the AED metabolism
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低剂量卡马西平和磺胺磺胺预用药背景下抗癫痫药物对角膜点燃小鼠癫痫发作影响的特点
的目标。本研究的目的是评估不同作用机制的抗癫痫药物(AED)在先前使用低剂量卡马西平和舒硫坦的背景下对小鼠角膜点燃模型的有效性。材料和方法。采用小鼠角膜点火模型。电刺激前30分钟,在卡马西平和磺胺平行预给药的情况下重现惊厥模型。研究了AED(磺胺、左乙拉西坦、卡马西平、丙戊酸盐、拉莫三嗪和雷加滨)在全身惊厥活动形成稳定综合征后的抗惊厥活性。结果和讨论。卡马西平和磺胺类药物可调节细胞色素P450酶系统的活性。因此,卡马西平在7和12 mg/kg剂量下无显著的抗惊厥活性(惊厥强度- 4.42±0.25点;(4.44±0.32分),对照组相同剂量卡马西平抗惊厥作用显著(3.52±0.26分;分别为3.2±0.6分)。初步慢性给予细胞色素P450系统诱导剂(卡马西平)和抑制剂(磺胺)时,拉莫三嗪的抗惊厥活性发生改变。在长期服用卡马西平和硫磺胺的背景下,观察到AED药理作用的变化,在我们看来,可能是由于细胞色素P450系统和参与AED代谢的其他酶组的调节
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来源期刊
ScienceRise: Pharmaceutical Science
ScienceRise: Pharmaceutical Science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.70
自引率
0.00%
发文量
39
审稿时长
6 weeks
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